Autosomal recessive hereditary disorder
Hereditary von Willebrand disease type 2
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Hereditary von Willebrand disease type 2N (disorder)
Hereditary von Willebrand disease type 2N
von Willebrand disease type 2N
Id359732009
StatusPrimitive
Has interpretationAbnormal
InterpretsHemostatic function
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD68.0
TermZiekte van Willebrand
SNOMED CT to ICD-10 extended map
TargetD68.0
RuleTRUE
AdviceALWAYS D68.0
CorrelationSNOMED CT source code to target map code correlation not specified